| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31459295-31459503 | Common:1; Rare:88 | ||||
| chr16:31472113-31472182 | Rare:16 | ||||
| chr16:31508351-31508484 | Common:2; Rare:57 | ||||
| chr16:46689134-46689381 | Common:1; Rare:88; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689518-46689714 | Common:2; Rare:82; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46973585-46973801 | Rare:98 | ||||
| chr16:47461012-47461374 | Common:2; Rare:144; Clinvar (benign):2 | ||||
| chr16:48091212-48091480 | Common:1; Rare:60 | ||||
| chr16:50065872-50066016 | Common:2; Rare:51 | ||||
| chr16:51151223-51151405 | Common:1; Rare:63 | ||||
| chr16:53208368-53208525 | Rare:29 | ||||
| chr16:53434378-53434502 | Common:1; Rare:35 | ||||
| chr16:53703809-53704223 | Common:1; Rare:132; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:56191071-56191556 | Common:5; Rare:167 | ||||
| chr16:56191615-56191699 | Rare:17 |